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Completed

NCT Number: NCT02717338

Blood Donor Competence, Autonomy and Relatedness Enhancement

The purpose of this study is to determine whether enhancing blood donor competence, autonomy, and/or relatedness increases intrinsic motivation to donate and improves donor retention.

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Key information

Conditions

Age range

16 year–24 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Ohio University

Athens, Ohio, 45701, United States

About this study

For health, safety, and economic reasons there is a critical need for novel approaches to enhance the retention of new blood donors. The current study examines an innovative, theory-driven approach to retention by promoting intrinsic motivation to donate again among new blood donors. Self-determination theory (SDT) proposes that people are more likely to persist with behaviors that are internally versus externally motivated, and considerable research supports the notion that more internalized motivation is associated with better adherence in a variety of health contexts. Similar findings have also been reported in the blood donation context where measures of the extent to which a donor identity has been internalized are positively related to both donation intention and future donation behavior. Based on prior work, the investigators propose to test a multi-component intervention designed to enhance one, two, or all three of the fundamental human needs that contribute to internal motivation according to SDT (i.e., competence, autonomy, relatedness). Using a full factorial design, first-time donors will be randomly assigned to a control condition or an intervention that addresses one, two, or all three of the fundamental needs. The primary aim is to determine whether the intervention conditions, alone and in combination, increase the likelihood of a donation attempt in the next year. The second aim is to examine intervention-specific increases in competence, autonomy, and relatedness as potential mediators of enhanced donor retention. Finally, an exploratory aim will examine an integrative model of motivation that views autonomy as a mediating influence on the more proximal, situational-level determinants of behavior (i.e., attitude, subjective norm, perceived behavioral control, and intention).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • First-time whole blood donor with New York Blood Center;
  • Eligible to donate again;
  • Willing to be randomly assigned;
  • Have, or be willing to establish, an active Facebook account.

Exclusion criteria

  • History of more than one lifetime whole blood donation (with any blood center);
  • Ineligible to donate again (based on New York Blood Center donor eligibility determination);
  • Unwilling to be randomly assigned;
  • Unwilling to sign up for closed Facebook group, if randomly assigned.

Treatment and study plan

Competence

Behavioral

Participants will be assigned to review our donor coping website that combines text, videos, and interactive features to directly address common donor fears and to offer advice on empirically-validated strategies to reduce fear, pain, and syncopal reactions.

Autonomy

Behavioral

Participants will be assigned to receive a brief telephone interview that we have developed that encourages blood donors to reflect upon their unique motivations for giving and how the act of donating is consistent with their broader life goals and values.

Relatedness

Behavioral

Participants will be asked to join a closed Facebook group for one month. The group encourages participants to discuss their experiences with blood donation, including such things as posting images of their donations and/or reasons for donating. Posts will be designed to encourage social interaction around donation experiences, identity formation and group affiliation.

Primary outcomes

  1. Repeat Blood Donation Attempts

    Time frame: one year plus 8 weeks post-initial donation

    Donor records will be used to track all instances of subsequent donation attempts during the one-year follow-up.

Secondary outcomes

  1. Blood Donation Attitude

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  2. Blood Donation Subjective Norms

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  3. Blood Donation Perceived Behavioral Control

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  4. Blood Donation Intention

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  5. Blood Donation Personal Moral Norm

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  6. Blood Donation Anticipated Regret

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  7. Donation Anxiety

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  8. Decisional Balance Inventory for Blood Donation

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  9. Blood Donation Ambivalence Scale

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  10. Blood Donor Identity Survey

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  11. Blood Donor Action and Coping Self-Efficacy

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  12. Blood Donor Relatedness Scale

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  13. Social Media Use Scale

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

  14. Social Media Relatedness Scale

    Time frame: Pre-intervention (requested 1-2 weeks post-donation) and Post-intervention (requested 7 weeks post-donation)

    Participant receives email request to complete online questionnaire at specified times.

Sponsors and collaborators

Lead sponsor

Ohio University

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • New York Blood Center

Registry information

Official study title

Blood Donor Competence, Autonomy and Relatedness Enhancement (Blood Donor CARE)

Important dates

Study start
2016
Primary completion
2020
Study completion
2020
First posted
Mar 23, 2016
Registry last updated
Mar 3, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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